https://lionessofjudah.substack.com/p/bill-gates-and-usaid-a-dangerous?

Bill Gates and USAID: A Dangerous Alliance With Deadly Secrets

Bill Gates has urged the Trump administration to reconsider its stance on USAID, calling it “an unbelievable asset” and warning that cuts could risk “millions” of lives.

By Ilya Tsukanov February 19, 2025

Bill Gates has urged the Trump administration to reconsider its stance on USAID, calling it “an unbelievable asset” and warning that cuts could risk “millions” of lives. What is the Microsoft mogul-turned billionaire ‘philanthropist’ really worried about?

USAID and the Gates Foundation have worked together for nearly 25 years on issues near and dear to Mr. Gates’ heart, from infectious diseases and vaccines to family planning, agriculture, and climate change.

Major collaborations include the Global Fund to Fight AIDS, Tuberculosis, and Malaria, and the Global Alliance for Vaccines and Immunization (GAVI).

Gates has also partnered with USAID on the Global Health Initiative and the Coalition for Epidemic Preparedness Innovations (CEPI).

If these names ring a bill, they should:

GAVI is running an ambitious program to vaccinate 86 million adolescent girls in developing countries against HPV with jabs including Gardasil, made by Merck, which now faces a lawsuit in the US over side effects ranging from sporadic paralysis to cancer.

Gates and USAID have continued supporting GAVI despite evidence from India starting in 2009 that its HPV jabs can cause severe illness or even death.

USAID committed over $2 billionto GAVI from 2001-2017, and $1.16 billion morebetween 2020-2023.

Leaked docs published by Revolver News in 2022 exposed a USAID scheme using pandemic funds for “reproductive health” (i.e. population control) in Africa.

CEPI, together with Anthony Fauci’s National Institutes of Health and the Food and Drug Administration, has been linked to controversial health schemes of its own, from a September 2019 workshop on vaccine biomarkers to partnership in Event 201, a pandemic simulation held in October 2019, just weeks before COVID hit.  (See link for article)

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**Comment**

If anything is named in the same sentence with Bill Gates, that’s all you need to know.

Gates has his fingers in so many pies it’s hard to keep them all straight.  The many pies include but aren’t limited to:

Bill Gates is everywhere, affecting everything, but he’s no philanthropist.

US Right to know exposed that USAID’s AGRA initiative is really all about chemical-laced monoculture farming, increased dependency and agrobusiness influence instead of reducing hunger.

WikiLeaks has already exposed USAID-Internews Network Censorship Psyop, which paid nearly a half a BILLION tax dollars to a secretive NGO operating a global news propaganda matrix deployed against taxpayers. 

It’s also been called a money laundering CIA front, with unelected bureaucrats who have zero oversight and accountability, which has not only funded the war in Ukraine, but has given:

  • Money to CIA
  • Money to WEF
  • Money to EcoHealth Alliance ($207 MILLION between 2009-2019) & Wuhan Lab for bioweapons research
  • Money to Bill Gates’ GAVI
  • Money to Soros-affiliated NGOs  (The East-West Management Institute, a beneficiary of both USAID and Soros’s Open Society Foundations (OSF), was granted over $260 million in tax-dollars)
  • Money for censorship in Europe and globally including the U.S. (BBC Media Action, Trusted News Initiative, etc. working along side Meta, Google, Microsoft, and Twitter/X using censorship/’fact checking’ under the guise of ‘misinformation’).  Did you know your tax dollars fund foreign media?
  • Money ($797 MILLION) to NGO’s in Guatemala funding child trafficking (over 190,052 children – over 3% of all children in Guatemala) and another 2 MILLION for sex changes in Guatemala.
  • Money to Afghanistan, Syria, Yemen, Gaza, and money to support electric vehicles in Vietnam, a transgender clinic in India, and:
    • $1.5 MILLION to a Serbian LGBT group
    • $1.5 MILLION to promote LGBT advocacy in Jamaica
    • $3.9 MLLION for LGBT causes in Macedonia
    • $1.5 MILLION to Belarus to promote art with people with disabilities
    • $164 MILLION for global radical organizations
    • $7.9 MILLION to Sri Lanka to avoid binary gender
    • 4.5 Million to combat ‘disinformation’ in Kazakastan
    • $10 MILLION to an Al-Qaeda linked terrorist group  Source
    • $17 BILLION to Ukraine, 3 BILLION to Israel, $733 MILLION to Yemen for 2023 alone.
  • USIAD has 10,000 employees and the organization gives away 40 BILLION yearly.

Note the following:

  • $20M for Iraqi Sesame Street
  • $2M for Moroccan pottery classes
  • $11M to tell Vietnam stop burning trash
  • $27M to give gift bags to illegals
  • $330M to help Afghanis grow crops
  • $300M on unused Afghani power plant
  • $200M on unused Afghani dam
  • $250M on unused Afghani road
  • 9 out of 10 media outlets in Ukraine rely on USAID funding

“We gave Syrians nine mil for humanitarian aid, but someone messed up and it went to Al Qaeda. We gave millions for bat research in Wuhan. USAID was funding fashion week in Paris. USAID is a $40 billion deep state social justice slush fund.” ~ Jesse Watters

See this important 4 min video on USAID, as well as this 9 min video with USAID expert Mike Benz, Executive Director of the Foundation for Freedom Online.

Gates isn’t worried about humanitarian causes.  He’s worried his blank check will end.

Don’t ever forget his father was a eugenicist and the head of Planned Parenthood.  Gates, like his father, firmly believes that ‘sustainability’ is dependent upon maintaining population control – which also just happens to be central to ‘climate change.’

Let’s be bloody honest – he wants a bunch of people to die, and he wants to decide just who dies.

The Kenyan Catholic Doctors Association and the Kenyan Catholic Bishops Conference issued a statement expressing concern that a UNICEF/WHO Tetanus vaccine was tainted with hCG, a contraceptive hormone. While this accusation has been denied by the agencies involved, the groups remain wary.

Gates scratches USAID’s back and return USAID scratches his back.

For more:

UPDATE:

Please also read:  Cordyceps Mushroom Holds Promise Against mRNA Vaccine-Induced Turbo Cancer

https://www.thefocalpoints.com/p/the-remarkable-anti-cancer-potential?

The Remarkable Anti-Cancer Potential of Mushrooms

Biological mechanisms, epidemiological evidence, and clinical data support the use of mushrooms in cancer prevention and treatment.

by Nicolas Hulscher, MPH

Recently, the entire MAHA movement was rightfully up-in-arms when Oracle’s Executive Chairman and Chief Technology Officer, Larry Ellison, pushed AI-generated cancer mRNA injections developed in 48 hours. The health freedom movement has grown tired of experimental gene therapies and seek safer, more natural approaches to cancer prevention and treatment. Dr. John Catanzaro, founder of Neo7Bioscience, has demonstrated the potential of precision-engineered peptides and small molecules for personalized cancer care. Dr. William Makis and many others advocate for the use of Ivermectin and Fenbendazole in cancer treatment, which has shown extreme promise. Another promising but often overlooked approach in Western Medicine is the use of mushrooms for cancer. In this article, I will summarize the biological mechanisms, epidemiological evidence, and clinical data supporting the use of mushrooms in cancer prevention and treatment.

Biological Mechanisms

Pathak et al reviewed the immunomodulatory effect of mushrooms and their bioactive compounds in cancer:

  • Immunomodulation: Mushroom bioactive compounds, such as lentinan, schizophyllan, and maitake-D fraction, stimulate the immune system by activating macrophages, dendritic cells, and natural killer (NK) cells, enhancing cytokine production (e.g., IL-2, IL-6, TNF-α) and increasing anti-tumor immune responses​.
  • Cell Cycle Arrest: Polysaccharides and other phytochemicals in mushrooms can halt cancer cell division at key regulatory checkpoints, particularly the G0/G1 and G2/M phases, thereby preventing tumor proliferation​.
  • Apoptosis Induction: Mushrooms trigger programmed cell death (apoptosis) in cancer cells via both the intrinsic (mitochondrial) and extrinsic (death receptor) pathways, leading to DNA fragmentation and caspase activation, effectively eliminating malignant cells​.
  • Angiogenesis Inhibition: Certain mushrooms, such as Ganoderma lucidum and Phellinus linteus, block the formation of new blood vessels (angiogenesis) that tumors need for growth by downregulating VEGF (vascular endothelial growth factor) and inhibiting endothelial cell proliferation​.
  • Oxidative Stress Regulation: Mushroom compounds like ergothioneine, glutathione, and polyphenols neutralize reactive oxygen species (ROS), reducing oxidative DNA damage that contributes to carcinogenesis​.  (See link for article)

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For more:

https://www.lymedisease.org/holly-ahern-australian-senate/

Prof. Holly Ahern’s Lyme disease comments to Australian Senate

2/5/25

The Australian Senate has launched an inquiry into the access to diagnosis and treatment for people in Australia with tick-borne diseases. Professor Holly Ahern of the United States recently submitted the following written comments and was also asked to give verbal remarks. (See video at end of this article.)

Dear Committee Members:

I am a scientist, professor of microbiology, and co-founder of a Lyme disease advocacy organization in New York State. I am also the Scientific Advisor for the Focus on Lyme Foundation in Arizona, which has funded research on several projects directed at improving the state of diagnostic testing for Lyme disease and other tick-borne illnesses.

I have served on several state and federal committees convened to address the growing problem of tick-borne diseases in the United States, most recently the 2022 Dept. of Health and Human Services, Tick Borne Disease Working Group (TBDWG).

But most of all, I am mother of a daughter who went from a record setting collegiate All American swimmer to bed bound and disabled over the course of only a few weeks. She lost years of her life as a result of flawed medical guidelines that prioritize care for patients early in the infection, while providing only minimal guidance for the diagnosis and care of patients in later stages of the disease.

In my daughter’s case, we saw the tick bite but she developed no rash. Fever, profound fatigue, widespread pain, and other symptoms began months later, and were attributed to a viral illness. The difficulties we faced in getting her illness diagnosed and appropriately treated in 2010 match those of hundreds of thousands of other people with Lyme disease in the United States and Europe, and also in Australia.

Biologically complex organism

Lyme disease is a bacterial infection caused by a microbe with global distribution. They are transmitted to humans by several species of tick. The bacteria are biologically complex. They adapt and survive in environments that would kill most other bacteria.

During human infection, some subgroups (genospecies) of these bacteria linger in the bloodstream, while others disseminate to connective tissue-rich areas of the body. Regardless, infection triggers profound immune system and other physiological events, leading to a wide range of symptoms that vary significantly among patients and can be quite severe.

The standard medical definition implies that the overwhelming majority of Lyme borreliosis (Lyme disease) patients are infected with the same bacteria and have the same uniform disease presentation, which is straightforward to diagnose and treat. As defined, Lyme disease is caused by only a few specific genospecies of Borrelia (now named Borreliella). Several other genospecies of Borrelia are associated with diseases collectively referred to as “Relapsing Fever borreliosis.”

Differences between the two diseases are subtle. Relapsing Fever Borrelia fail to produce the skin manifestation (erythema migrans or “bull’s-eye” rash) that is noted in Lyme disease; however, other symptoms are very similar. Existing diagnostic tests for Lyme disease don’t detect infections caused by Relapsing Fever Borrelia.

Thus, a patient may be bitten by a tick and infected with a Relapsing Fever Borrelia, such as B. miyamatoi, show all the symptoms that a patient with Lyme disease would have, but may not be diagnosed or treated for the infection because the EM rash did not appear and/or the standard lab tests for Lyme disease were negative.  (See link for article)

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For more:

https://immunetolerance.substack.com/p/the-biosecurity-ethics-and-immune?

The Biosecurity Ethics & Immune Tolerance Awareness Initiative

Welcome to the Substack to raise awareness of #ImmuneTolerance and #VaccineInjuries #chronicdisease #autism #mentalillness #ADD #ADHD

Welcome to the Substack of the Biosecurity Ethics and Immune Tolerance Awareness Initiative. The Biosecurity Ethics & Immune Tolerance Awareness Initiative exists to educating the public about the role of immune tolerance in chronic diseases, neurological and neuropsychiatric disorders, and cancers. We further educate and advocate for ethical biosecurity practices and informed policy decisions made in full transparency, through ethical guidelines, working to close critical vulnerabilities, and defend actual national security from foreign influence in public health and biodefense strategies, rather than using National Security as guise to hide scandals and evade accountability.

The Truth of Chronic Disease in America Shall be Unveiled. The Health of All Depends on it.

In 1960, the science of slow, chronic disease and persistent infections, once baptized “immune tolerance” was obscured and marginalized to the realm of organ transplantation and its recipients, as the 1960 Nobel Prize was given in error to Frances MacFarland Burnet and Peter Medawar for immune tolerance through organ transplantation even though the two never worked together nor were they nominated together by anyone. However, it was Erich Traub, who had discovered it in 1935 through his discovery of Lymphocytic Choriomeningitis Virus (LCM) in white mice.

Immune tolerance is a term applied to the state of chronic suppression of the immune system, where the immune system is too overwhelmed to adequately fight back. It is specifically defined as :

A state of unresponsiveness to a specific antigen or group of antigens to which a person is normally responsive. Immune tolerance is achieved under conditions that suppress the immune reaction and is not just the absence of an immune response.

This same condition correlated to another phenomenon alternatively coined “immune paralysis” following injection of large doses of pneumococcal polysaccharide antigens. In short, immune tolerance is immune paralysis. This was a major finding that would have vastly changed our understanding of chronic disease and immunology, yet the scientific establishment ignored it and marginalized it to organ transplantation, because the same condition is also seen in organ transplant recipients, and this is also thought to be the result of antigenic stimuli. Attributing it to organ transplantation only totally ignores something so immensely important about immunology and the disease process that it might as well be considered one of the pillars of chronic disease showing that unlike acute diseases measured by heavy inflammation and immune response, there is a polar opposite side of disease, measured by immunosuppression, lack of visible inflammation, and chronic disease.

However, the Nobel Prize “given in error” appears more likely to have been a deliberate choice as it would have devastated Western immunology and the science of infectious disease determined by antibodies and observable inflammation. Equally so, it would have flipped vaccine science on its head and exposed the true nature of vaccine-induced “immunity” as a slow destruction of the immune system rather than building it up as strong and healthy.

Erich Traub first elucidated the condition during vaccine research at the Rockefeller Institute in 1935 when he injected the brains of mice with foreign proteins, reactivating dormant LCM virus from within the mice, causing an epidemic from scratch. The result was a slow chronic disease via immunosuppression and persistent viral infection that could be passed congenitally from mother to newborn, maintaining itself through generations, while silently degenerating the genetic integrity of subsequent generations, plaguing them with chronic disease, neurological syndromes/wasting disease, and cancer.

In short, antigenic stimuli were behind this condition which produced chronic immunodeficiency and reactivated dormant viruses from within the body, invited additional opportunistic infections to create a highly complex and complicated chronic disease accompanied by neurological/neuropsychiatric disorders, wasting disease, and cancer. It would present in the absence of detectable antibodies and little to no outward inflammation. Likewise, Traub’s experiments demonstrate how a vaccine antigen too toxic for the body can cause new outbreaks with other diseases already dormant in the vaccine recipient.

Since the 1960s when the infectious origins of immune tolerance were buried and obscured, the science of chronic disease and neurological/neuropsychiatric disorders began working in reverse. Public Health has been ignoring the underlying condition at the root of these diseases for decades by using tests and diagnostics that evade the evidence of the condition by using the wrong biomarkers of disease and calling it “evidence-based medicine. This so-called Evidence-based medicine only uses antibody response and inflammation as its criteria for diagnosis but immune tolerance is the polar opposite. There are ways to detect and diagnose immune tolerance using other biomarkers, but these are very different than biomarkers used to study acute diseases marked by robust antibody response and heavy inflammation. By using inadequate biomarkers like antibodies and acute inflammation as criteria for diagnosis, this will invariably show nothing of value for diagnosing a disease that is marked by immune tolerance outcomes and as a result, no disease will be recorded.   (See link for article)

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**Comment**

Important quote:

Nowhere is this more apparent than the recent wave of sick people injured by the COVID-19 vaccine.

Mandatory reading for each and every Lyme/MSIDS patient and every person who still believes in ‘vaccines.’

This, right here, is the pearl that has been trampled on by public health and mainstream medicine.

Yale scientists have found T-cell exhaustion and prolonged spike protein production in some COVID shot recipients with spike levels increasing over time leading to post-vaccine brain fog and immune dysfunction. Finally, someone is connecting the dots between ‘long COVID’ and post vaccination syndrome.  Findings Suggest Immune Imbalances and Viral Reactivation May Contribute to Chronic Symptoms After COVID-19 Vaccination.

But mainstream medical journals won’t publish it.

The variety of symptoms include:

  • Excessive fatigue (85%)

  • Tingling/numbness (80%)

  • Exercise intolerance (80%)

  • Brain fog (77.5%)

  • Difficulty concentrating (72.5%)

  • Sleep disturbances (70%)

  • Neuropathy (70%)

  • Muscle aches (70%)

  • Anxiety (65%)

  • Tinnitus (60%)

  • Burning sensations (57.5%)​

Immunosuppression can be caused by vaccinations of all kinds as well as unethical biodefense practices using simulants in open-air tests since the 50’s.  Finnegan states:

Lyme disease had been one such simulant spread through ticks on shorebirds in the early 1950s under the supervision of Erich Traub on Plum Island, using strains of Borrelia anserina that he had acquired from Rockefeller-funded psychiatrist Franz Jahnel through his student Werner Schäfer in 1939.

Finnegan goes on with the sordid history of immune tolerance and how public health officials understand it fully and are deliberately using it as a defense strategy, while misleading the public.

Certain antigens responsible for immune tolerance are also potent mitogens which are responsible for cancer through the upregulation of telomerase.

MAHA will fail if the origins of immune tolerance via toxic antigen is not addressed.

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“If we had surveyed the public two years ago, would you be willing to take a genome cell therapy and inject it into your body, we would have probably had a 95% refusal rate.” ~ Dr. Oelrich

Now injections will probably become a thing of the past as airborne mRNA ‘vaccines’ are being created that can be delivered straight into the lungs without a shot.

https://www.thefocalpoints.com/p/gravy-train-of-nih-indirects-gets?

Gravy Train of NIH “Indirects” Gets Bull-DOGEd

Progressively Growing Extra Costs Tagged to Research Grants Cut Back to 15%

By Peter A. McCullough, MD, MPH

I talked to someone today who has recently received a coveted NIH RO1 grant. Instead of being happy she said she is terrified. Why? Recently, Elon Musk and the Department of Government Efficiency (DOGE) has trimmed back “indirects” universities and hospitals slap on top of the direct research funded projects. This rate has grown from 15% over decades to >50% at many prestigious medical centers. The current indirect rate at Harvard is 69%.  (See link for article)

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**Comment**

This website continually posts information on the unhealthy alliance between Industrygovernment, and University research facilities

For a great start, Congress needs to repeal the Bayh-Dole Act of 1980 so that the government agencies entrusted with public health do not have conflicts of interest in owning patents.  

Research institutions at universities should not be colluding with government by receiving government money.  The two need to be separate.

MAHA has begun, but there’s a lot to do.

The entire government grant process is riddled with conflicts: